Array-CGH detection of a de novo 0.7-Mb deletion in 19p13.13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms: Letters

Epilepsia

Volumn 50, Issue 11, 2009, Pages 2501-2503

  Auvin, Stéphane ^a,b   Holder Espinasse, Muriel ^b   Lamblin, Marie Dominique ^b   Andrieux, Joris ^b  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b LILLE UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CALCIUM CHANNEL ALPHA 1A; UNCLASSIFIED DRUG;

CASE REPORT; CHROMOSOME 19P; CLINICAL FEATURE; DISEASE ASSOCIATION; EPILEPSY; GENE DELETION; HUMAN; INFANTILE SPASM; LETTER; MALE; MENTAL DEFICIENCY; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT;

EID: 70350401137     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2009.02189.x     Document Type: Letter

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